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“CareFusion” V. Mueller Nonpowered neurosurgical instrument (Non-Sterile) - Taiwan Registration 018b2f560afa4cbca5a7405a75c7ea4f

Access comprehensive regulatory information for “CareFusion” V. Mueller Nonpowered neurosurgical instrument (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 018b2f560afa4cbca5a7405a75c7ea4f and manufactured by CareFusion. The authorized representative in Taiwan is BESPRING INTERNATIONAL MARKETING CO., LTD..

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018b2f560afa4cbca5a7405a75c7ea4f
Registration Details
Taiwan FDA Registration: 018b2f560afa4cbca5a7405a75c7ea4f
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Device Details

“CareFusion” V. Mueller Nonpowered neurosurgical instrument (Non-Sterile)
TW: “客愛福生”密米樂非動力式神經外科用器械 (未滅菌)
Risk Class 1
MD

Registration Details

018b2f560afa4cbca5a7405a75c7ea4f

Ministry of Health Medical Device Import No. 020166

DHA09402016606

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-powered Neurosurgical Devices (K.4535)".

K Devices for neuroscience

K4535 Non-powered neurosurgical instruments

Imported from abroad

Dates and Status

Mar 11, 2019

Mar 11, 2024